The emergence and re-emergence of plant diseases has increased noticeably in recent years. This has been attributed to climate change, monoculture and trade (Willocquet et al., 2020). An example is the occurrence of Xylella fastidiosa in different regions of the world (Almeida and Nunney, 2015). It was described as a “relatively obscure pathogen” in 2002 (Hopkins and Purcell, 2002), but 10 years later it is now considered a major threat to agriculture worldwide.
Xanthomonas species are members of the Lysobacteriaceae (previously known as Xanthomonaceae), a family within the class Gammaproteobacteria. They have an extremely wide host range, infecting both monocotyledonous and dicotyledonous plants. The number of first reports of novel Xanthomonas species or pathovars has increased in recent years (Bansai et al., 2022; Dia et al., 2022) as has the appearance of more aggressive strains of known species (Chen et al.). The same host has also been shown to harbor both pathogenic and non-pathogenic strains (Cesbron et al., 2015; Fernandes et al., 2021; Ramnarine et al., 2022). Furthermore, Xanthomonas species have been shown to have increased their host and geographic range (Curland et al., 2020; Sigillo et al., 2021). Horizontal gene transfer has been identified as one potential mechanism favouring host-range evolution (Chen et al., 2018).
Xanthomonas species can colonize novel hosts and inhabit unique ecological niches due to their extensive genomic diversity. This rich diversity has been shown to possibly be linked to different production systems (Abrahamian et al., 2019; Klein-Gordon et al., 2021) and cultivated regions (Chen et al., 2021). Xanthomonas species are also an important component of the plant, rhizosphere and soil microbiomes (da Silva et al., 2021). The ability of this species to infect novel hosts and occur in different regions of the world has led to an increased research on such topics as host-pathogen interactions, virulence and pathoadaption. There has also been an increased understanding of the ecology and epidemiology of these pathogens.
Differences in aggressiveness between strains of X. campestris pv. campestris to cabbage was recorded in China (Chen et al.). The genomes of aggressive and less aggressive strains were sequenced. Differences were noted in Type III secreted effector repertoires, virulence factors and secreted proteins. The authors thus found a direct correlation between genomic variability and virulence of X. campestris pv. campestris.
In China, two strains of X. oryzae pv. oryzae from two locations, low land and high mountain paddies, were shown to differ significantly in virulence (Li et al.). In a comparative genomic analysis, the strains differed in <10 genes, including a gene coding for the transcription activator-like effector (TALE). The tal genes were variable in both their number and sequence. This study thus highlighted the variability of TALEs genes in strains of X. oryzae pv. oryzae.
Bacterial spot, caused by four Xanthomonas species, is an important disease of tomatoes and peppers. Jibrin et al. identified a novel race (T5) in Nigeria which was shown to be the product of recombination between two of the four Xanthomonas species. Genomes of these species have only been sequenced from five African countries. The authors thus note that there is thus a lack of information on the evolution and biology of these pathogens on this continent which could provide a foundation for genome-informed host–pathogen and ecological interaction investigations that are novel to production systems in Africa.
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Acknowledgments
The authors would like to thank co-editors and the contributors to this Research Topic.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Summary
Keywords
geographic range, host range, virulence, aggressiveness, resistance
Citation
Coutinho TA, Jacques M-A and Jones J (2022) Editorial: Emergence and re-emergence of plant diseases caused by Xanthomonas species. Front. Microbiol. 13:1081601. doi: 10.3389/fmicb.2022.1081601
Received
27 October 2022
Accepted
15 November 2022
Published
12 December 2022
Volume
13 - 2022
Edited and reviewed by
Jesús Navas-Castillo, La Mayora Experimental Station (CSIC), Spain
Updates
Copyright
© 2022 Coutinho, Jacques and Jones.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Teresa A. Coutinho Teresa.Coutinho@up.ac.za
This article was submitted to Microbe and Virus Interactions with Plants, a section of the journal Frontiers in Microbiology
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.